Upregulation of MMP-13 and TIMP-1 expression in response to mechanical strain in MC3T3-E1 osteoblastic cells

被引：19

作者：

Li Y. ^{[1
]}

Tang L. ^{[1
]}

Duan Y. ^{[1
]}

Ding Y. ^{[1
]}

机构：

[1] Department of Orthodontics, College of Stomatology, Fourth Military Medical University, Xi'an

来源：

BMC Research Notes | / 3卷 / 1期

基金：

中国国家自然科学基金;

关键词：

Genistein; Mechanical Strain; Orthodontic Tooth Movement; Orthodontic Force; Cyclic Tensile Strain;

D O I：

10.1186/1756-0500-3-309

中图分类号：

学科分类号：

摘要：

Background. Mechanical strain plays a significant role in the regulation of bone matrix turnover, which is mediated in part by matrix metalloproteinase (MMP)-13 and tissue inhibitors of matrix metalloproteinase (TIMP)-1. However, little is known about the correlation between mechanical strain and osteoblastic cell activities, including extracellular matrix (ECM) metabolism. Herein, we determined the effect of different magnitudes of cyclic tensile strain (0%, 6%, 12%, and 18%) on MMP-13 and TIMP-1 mRNA and protein expression in MC3T3-E1 osteoblasts. Furthermore, we employed specific inhibitors to examine the role of distinct signal transduction pathways known to mediate cellular responses to mechanical strain. Results. We identified a magnitude-dependent increase in MMP-13 and TIMP-1 mRNA and protein levels in response to mechanical strains corresponding to 6%, 12%, and 18% elongation. The strain-induced increases in MMP-13 and TIMP-1 mRNA expression were inhibited by PD098059 and cycloheximide, respectively. Conclusions. Our results suggest a mechanism for the regulation of bone matrix metabolism mediated by the differential expression of MMP-13 and TIMP-1 in response to increasing magnitudes of mechanical strain. © 2010 Li et al; licensee BioMed Central Ltd.

引用

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